rs61735303
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs61735303(A;A) |
Make rs61735303(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 86952254 |
Gene | FZD4, PRSS23 |
is a | snp |
is | mentioned by |
dbSNP | rs61735303 |
dbSNP (classic) | rs61735303 |
ClinGen | rs61735303 |
ebi | rs61735303 |
HLI | rs61735303 |
Exac | rs61735303 |
Gnomad | rs61735303 |
Varsome | rs61735303 |
LitVar | rs61735303 |
Map | rs61735303 |
PheGenI | rs61735303 |
Biobank | rs61735303 |
1000 genomes | rs61735303 |
hgdp | rs61735303 |
ensembl | rs61735303 |
geneview | rs61735303 |
scholar | rs61735303 |
rs61735303 | |
pharmgkb | rs61735303 |
gwascentral | rs61735303 |
openSNP | rs61735303 |
23andMe | rs61735303 |
SNPshot | rs61735303 |
SNPdbe | rs61735303 |
MSV3d | rs61735303 |
GWAS Ctlg | rs61735303 |
GMAF | 0.0101 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs61735303(A;A) |
Alt | rs61735303(A;A) |
Reference | Rs61735303(G;G) |
Significance | Probable-non-pathogenic |
Disease | Familial exudative vitreoretinopathy not specified |
Variation | info |
Gene | PRSS23 FZD4 |
CLNDBN | Familial exudative vitreoretinopathy not specified |
Reversed | 0 |
HGVS | NC_000011.9:g.86663296G>A |
CLNSRC | |
CLNACC | RCV000368489.1, RCV000455735.1, |
[PMID 15223780] Spectrum and frequency of FZD4 mutations in familial exudative vitreoretinopathy.
[PMID 15733276] Genetic variants of frizzled-4 gene in familial exudative vitreoretinopathy and advanced retinopathy of prematurity.